Evidence map›Paper›PMID 32946753›Full record

ArticleCurrent biology : CB2020

Opposing, Polarity-Driven Nuclear Migrations Underpin Asymmetric Divisions to Pattern Arabidopsis Stomata.

Andrew Muroyama, Yan Gong, Dominique C Bergmann

Erratum issuedOpen access · hybridAbstract readVideo-Audio Media
In one paragraph

Article in Current biology : CB, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
11.1field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Cyclin' Through the Root: Developmental Control of Cell Cycle Progression in theAnnual review of cell and developmental biology · 2026
    Review
  3. Article
  4. Force-responsive symmetric cell divisions orient stomata along global tissue axes.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. A transient radial cortical microtubule array primes cell division inProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Review
  16. Article
  17. Article
  18. Asymmetric cell division in plant development.Journal of integrative plant biology · 2023
    Review
  19. Regulation of organelle size and organization during development.Seminars in cell & developmental biology · 2023
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Andrew MuroyamaDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Yan GongDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Dominique C BergmannDepartment of Biology, Stanford University, Stanford, CA 94305, USA; Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA. Electronic address: dbergmann@stanford.edu.
Stanford University · USHoward Hughes Medical Institute · US

Funding

Dynamic polarity mechanisms controlling stem cell asymmetry during tissue developmentF32GM133102 · NIGMS · STANFORD UNIVERSITY · PI MUROYAMA, ANDREW D · 2019 to 2020
$122k
Howard Hughes Medical InstituteNIGMS NIH HHS F32 GM133102
6 · The paper itself

Abstract

Multicellular development depends on generating and precisely positioning distinct cell types within tissues. During leaf development, pores in the epidermis called stomata are spaced at least one cell apart for optimal gas exchange. This pattern is primarily driven by iterative asymmetric cell divisions (ACDs) in stomatal progenitors, which generate most of the cells in the tissue. A plasma membrane-associated polarity crescent defined by BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE (BASL) and BREVIS RADIX family (BRXf) proteins is required for asymmetric divisions and proper stomatal pattern, but the cellular mechanisms that orient ACDs remain unclear. Here, utilizing long-term, quantitative time-lapse microscopy, we identified two oppositely oriented nuclear migrations that precede and succeed ACD during epidermal patterning. The pre- and post-division migrations are dependent on microtubules and actin, respectively, and the polarity crescent is the unifying landmark that is both necessary and sufficient to orient both nuclear migrations. We identified a specific and essential role for MYOXI-I in controlling post-ACD nuclear migration. Loss of MYOXI-I decreases stomatal density, owing to an inability to accurately orient a specific subset of ACDs. Taken together, our analyses revealed successive and polarity-driven nuclear migrations that regulate ACD orientation in the Arabidopsis stomatal lineage.

Indexed as

ArabidopsisArabidopsis ProteinsAsymmetric Cell DivisionCell Cycle ProteinsCell LineageCell NucleusCell PolarityIntravital MicroscopyMolecular Motor ProteinsPlants, Genetically ModifiedPlant StomataTime-Lapse ImagingArabidopsis ProteinsBASL protein, ArabidopsisBREVIS RADIX protein, ArabidopsisCell Cycle ProteinsMolecular Motor Proteinsmyosin XI-i protein, ArabidopsisArabidopsisasymmetric divisioncytoskeletonleaf developmentMYOXI-Inuclear migrationstomatatissue patterning

Identifiers

PMID32946753
PMCPMC7674273
OpenAlexW3087105745

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.